gudid
Primary ID: 122000700
SE3123 (UDI 122000700)
Manufactured by Esaote Europe B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SE3123 - Primary ID 122000700
Device Regulatory Overview
The SE3123 (Model/Catalog Number: 122000700) is a medical device manufactured by Esaote Europe B.V.. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 122000700
- Product Code / EMDN
- ITX
- Device Name
- Database Sync Date
- 2026-08-09 09:04:29
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SE3123?
The registered manufacturer of record for SE3123 is Esaote Europe B.V..
What is the Primary UDI-DI identifier for SE3123?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 122000700.
What classification code is assigned to this device?
This device is registered under product classification code ITX.
Similar Classification Devices (ITX)
Other Devices by Esaote Europe B.V.
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